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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477248Generated: November 2, 2026

Trimethylsilylacetylene → HCID 131736482, compound

https://huagongshe.com/reaction/1477248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 118659434HCID 118659434—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 131736482HCID 131736482168.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring suspension of methyl 4-(4-bromophenyl)-2-methyl-2-(methylsulfonyl)butanoate (9.3, 6.36 g, 18.23 mmol), bis(triphenylphosphine)palladium(II) chloride (1.28 mg, 1.82 mmol) and copper(I) iodide (347 mg, 1.82 mmol) in triethylamine (30 mL) was added ethynyltrimethylsilane (0.92 mL, 6.49 mmol) and the reaction mixture was heated to 80° C. briefly, and then allowed to stir at room temperature for 18 hr. Volatiles were removed under reduced pressure and the resulting residue was purified by flash chromatography (silica gel/15-50% EtOAc/hexanes) to yield methyl 2-methyl-2-(methylsulfonyl)-4-(4-((trimethylsilyl)ethynyl)phenyl)butanoate (9.4, 4.0 g, 59.9% yield). MS: m/z calcd for C18H26O4SSi 366.13. found [M+H]+ 367.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403758B2
Source datasetuspto-grants-2016_08
ORD IDord-94d212b5803743d39e15ed1c8ea5c158
Source noteuspto-grants-2016_08